1,6-Dibromonaphthalene

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CAS:19125-84-9
Purity:98% HPLC Package:5G;10G;25G;50G;100G;250G;1KG
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CAS:19125-84-9
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CAS:19125-84-9
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CAS:19125-84-9
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Products Intro: Product Name:1,6-Dibromonaphthalene
CAS:19125-84-9
Package:1g; 5g; 25g; 1kg; 5kg; 25kg

1,6-Dibromonaphthalene manufacturers

  • 1,6-Dibromonaphthalene
  • 1,6-Dibromonaphthalene pictures
  • $1.00 / 1KG
  • 2019-09-02
  • CAS:19125-84-9
  • Min. Order: 1KG
  • Purity: 98%
  • Supply Ability: 1lg; 2kg; 5kg; 10kg; 100kg
1,6-Dibromonaphthalene Basic information
Product Name:1,6-Dibromonaphthalene
Synonyms:1,6-Dibromonaphthalene;Naphthalene, 1,6-dibroMo-;1,6-Dibromonaphthalene - [D94626]
CAS:19125-84-9
MF:C10H6Br2
MW:285.96
EINECS:
Product Categories:
Mol File:19125-84-9.mol
1,6-Dibromonaphthalene Structure
1,6-Dibromonaphthalene Chemical Properties
storage temp. Sealed in dry,Room Temperature
AppearanceWhite to off-white Solid
InChIInChI=1S/C10H6Br2/c11-8-4-5-9-7(6-8)2-1-3-10(9)12/h1-6H
InChIKeyPUIAXCYSKMFFOU-UHFFFAOYSA-N
SMILESC1(Br)=C2C(C=C(Br)C=C2)=CC=C1
Safety Information
MSDS Information
1,6-Dibromonaphthalene Usage And Synthesis
Chemical Properties1,6-Dibromonaphthalene is a white crystalline solid that has two isomers.
Uses1,6-Dibromonaphthalene is mainly used as a pharmaceutical intermediate. It can be used as a ligand for metal ions, such as copper, iron, and zinc. It has also been shown to have selectivities for unsymmetrical molecules with unmodified organic ligands.
Synthesis
1,6-Dihydroxynaphthalene

575-44-0

1,6-Dibromonaphthalene

19125-84-9

Example 20: Preparation of Compound 50; [235] [236] 20-A. Preparation of Compound 20a; To a solution of 1,6-dihydroxynaphthalene (1.2 g, 7.68 mmol) in acetonitrile (50 mL) was added phosphorus tribromide (PBr3, 2.9 g, 10.8 mmol), and the mixture was heated and refluxed with stirring for 48 hours. Upon completion of the reaction, the mixture was cooled to room temperature, followed by the addition of methanol (100 mL) to precipitate the solid product. The solid was collected by filtration, washed well with methanol and dried under reduced pressure to afford compound 20a 1,6-dibromonaphthalene (1.6 g, 74% yield). [M] = 286

References[1] Patent: WO2007/86695, 2007, A1. Location in patent: Page/Page column 76-77
[2] Bioorganic and Medicinal Chemistry Letters, 2008, vol. 18, # 1, p. 267 - 273
1,6-Dibromonaphthalene Preparation Products And Raw materials
Raw materials1,6-Dihydroxynaphthalene-->Phosphorus tribromide-->Acetonitrile
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